Allele Registry

Canonical Allele Identifier: PA2825941889

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058619

RCV000183188

ClinVar Variation:

67840

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Ala1325Ser	CA017686 NM_001160160.2:c.3973G>T